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Multiprofessional follow-up programmes are needed to address psychosocial, neurocognitive and educational issues in children with brain tumours

机译:需要多专业的跟进计划来解决脑肿瘤儿童的社会心理,神经认知和教育问题

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摘要

AIM: The aim of this study was to coordinate the structured psychosocial, neurocognitive and educational follow-up of children treated for brain tumours with the medical protocol and apply the model in two Swedish healthcare regions. METHODS: We invited all children living in the two regions, who had been diagnosed with a brain tumour from October 1, 2010, through June 30, 2012, to participate along with their parents. The follow-up programme evaluated the emotional status of the parents and patients and assessed the children's general cognitive level, working memory, speed of performance, executive functions and academic achievement from diagnosis through to adult care. RESULTS: During the study period, 61 children up to the age of 17.1 years were diagnosed with a brain tumour, but 18 of these were excluded for various reasons. The majority of the mothers (70%) displayed significantly poor emotional status, as did 34% of the fathers and 21% of the children. The majority of the children (57%) also showed poor neurocognitive performance and needed special adaptations at school (66%). CONCLUSION: Our findings indicate the need for coordinated, multiprofessional follow-up programmes, well anchored in the healthcare organisation, for children diagnosed with brain tumours.
机译:目的:本研究的目的是根据医学方案协调对接受脑瘤治疗的儿童的结构化社会心理,神经认知和教育随访,并将该模型应用于两个瑞典医疗保健地区。方法:我们邀请了居住在这两个地区的所有儿童(与2010年10月1日至2012年6月30日之间被诊断出患有脑瘤)一起与父母一同参加。后续计划评估了父母和患者的情绪状况,并评估了儿童的总体认知水平,工作记忆,表现速度,执行功能和从诊断到成人护理的学业成绩。结果:在研究期间,有61名年龄在17.1岁以下的儿童被诊断出患有脑肿瘤,但出于各种原因将其中18名儿童排除在外。大多数母亲(70%)表现出明显的不良情绪状态,父亲,儿童中有34%,儿童中有21%。大多数儿童(57%)也表现出较差的神经认知能力,需要在学校进行特殊适应(66%)。结论:我们的发现表明,对于诊断为脑肿瘤的儿童,需要在医疗保健组织中扎根的协调,多专业的跟踪计划。

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